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clinical dysmorphology

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Indexaciones
ncbi
Nombre Corto clin dysmorphol
Nombre Abreviado clin dysmorphol
ISSN 1473-5717
Objetivo y Alcance
URL
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Publications Per Year

Recent Articles (1 total)

2020
A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndrome.
Guzoglu, Nilufer;Aslan, Mustafa K;Gunay, Yasemin D;Atasoy, Pinar;Ceylaner, Serdar;Aliefendioglu, Didem;
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